Canonical Allele Identifier: CA2242998124
Gene: MIR22HG HGNC NCBI

Linked Data

dbSNP Id: rs1914432730
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715028A>T , CM000679.2:g.1715028A>T GRCh38
NC_000017.10:g.1618322A>T , CM000679.1:g.1618322A>T GRCh37
NC_000017.9:g.1565072A>T NCBI36
NG_032811.1:g.3506A>T

Transcript Alleles

HGVS Amino-acid Change
NR_028502.1:n.144-1014T>A
NR_028503.1:n.144-1014T>A
NR_028504.1:n.144-575T>A
NR_028505.1:n.144-1014T>A
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